Cosmedix SPF50

Product NDC
61531-103
11-digit product format
615310103
Labeler code
61531
Product ID
61531-103_7cc718a7-7756-4013-b54d-dc1a0b1e4e6f
Type
HUMAN OTC DRUG
Nonproprietary name
Sunscreen
Dosage form
EMULSION
Route
TOPICAL
Labeler
Universal Packaging Systems, Inc. DBA: PakLab
Application
part352
Marketing category
OTC MONOGRAPH FINAL
Marketing start
2015-11-24
Marketing end
0000-00-00
Substance
OXYBENZONE; OCTINOXATE; AVOBENZONE; OCTISALATE
Active strength
0 g/g; g/g; g/g; g/g
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
61531-103-012021-07-23C16284748780-1c7ccaba7-12ba-fd44-e053-dadaa90aa01b2552a16c-ea57-64a3-e054-00144ff8d46c

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
61531-103-01Cosmedix SPF5050 g in 1 TUBEEMULSION502

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
61531-103COSMEDIX SPF50 (SUNSCREEN) EMULSION [UNIVERSAL PACKAGING SYSTEMS, INC. DBA: PAKLAB]2Legacy NDC, 1 package rows20191228_2552a16c-ea57-64a3-e054-00144ff8d46c.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
61531-103-016153101030150 g in 1 TUBE (61531-103-01) 50 g2015-11-240000-00-00NoNoCurrent